Business Analysis

IS YOUR ROLE BUSINESS ANALYSIS?

As a Business Analyst, you are critical in choosing the right labeling solution. You are in a unique position of researching, understanding and recommending the overarching infrastructure of the required solution, along with its challenges and opportunities.

It is your responsibility to convey these findings to key stakeholders.

We provide not only a configurable labeling solution that enables you to meet all the requirements of the project, but we also have our internal experts ready to discuss any specific needs. Our in-house teams can support you with validation and compliance through project planning, risk assessment, testing implementations and supply full documentation.

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“We knew what level of quality we required and the PRISYM system not only delivered, but exceeded our expectations. Unlike PRISYM, many of the other systems we considered did not provide the correct level of service and security, which is an especially important factor in our industry. Plus, the PRISYM ID’s labeling software is user-friendly and has a very useful reminder mechanism.”

CHOSEN BY THESE CUSTOMERS...

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OFFERING THE PERFECT OPTION FOR YOU

LABELING SOFTWARE

Labeling Software icon - Business AnalysisLabel and Artwork Management Solution for Medical Device, Clinical Trials and Pharmaceutical sectors.

DEPLOYMENT

Deployment icon 02 - Business AnalysisWe offer tiers of deployment to suit your needs and size of the business. But our offer is much more than just deployment.

SERVICES

Services icon - Business AnalysisWe are the only software vendor in life science industry who supplies in- house validation documentation and implementation support.

BUSINESS ANALYSIS LABELING RESOURCES

EU MDR Infographic 10 Sticking points Infographic - Business Analysis Medical Device Label Before and After EU MDR – 10 Sticking Points Posted in: Achieving Regulatory Compliance, Business Analysis, Infographic Archives, Medical Device, Operations & Labeling, Project Managers, Regulatory & Compliance -

EU MDR introduces additional information that needs to be included on labels, forcing organizations to design new label templates that make room for data not previously part of the labeling system.

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